Ru-Catalyzed C–H alkenylation on the arene ring of pirfenidone using pyridone as a directing group

null Raziullah; Mohit Kumar; Ashfaq Ahmad; Himangsu Sekhar Dutta; Anushka Rastogi; Manoj Kumar Gangwar; Dipankar Koley

doi:10.1039/d2cc00257d

Ru-Catalyzed C–H alkenylation on the arene ring of pirfenidone using pyridone as a directing group

Raziullah, Mohit Kumar, Ashfaq Ahmad, Himangsu Sekhar Dutta, Anushka Rastogi, Manoj Kumar Gangwar, Dipankar Koley

Physical Sciences and Engineering

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

A method to functionalize the arene ring of pirfenidone has been demonstrated using pyridone as a directing group.

Original language	English (US)
Pages (from-to)	3481-3484
Number of pages	4
Journal	Chemical Communications
Volume	58
Issue number	21
DOIs	https://doi.org/10.1039/d2cc00257d
State	Published - Feb 22 2022

Bibliographical note

KAUST Repository Item: Exported on 2023-01-12
Acknowledgements: We gratefully acknowledge DST-SERB (EMR/2016/000613) for Financial support, CSIR-New Delhi (H. S. D., A. A., A. R.), and UGC-New Delhi (M. K., R.). We thank the CDRI SAIF division for analytical support. CDRI Communication No 10364.

ASJC Scopus subject areas

Materials Chemistry
Surfaces, Coatings and Films
Metals and Alloys
Ceramics and Composites
General Chemistry
Catalysis
Electronic, Optical and Magnetic Materials

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10.1039/d2cc00257d

Cite this

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title = "Ru-Catalyzed C–H alkenylation on the arene ring of pirfenidone using pyridone as a directing group",

abstract = "A method to functionalize the arene ring of pirfenidone has been demonstrated using pyridone as a directing group.",

author = "Raziullah and Mohit Kumar and Ashfaq Ahmad and Dutta, {Himangsu Sekhar} and Anushka Rastogi and Gangwar, {Manoj Kumar} and Dipankar Koley",

note = "KAUST Repository Item: Exported on 2023-01-12 Acknowledgements: We gratefully acknowledge DST-SERB (EMR/2016/000613) for Financial support, CSIR-New Delhi (H. S. D., A. A., A. R.), and UGC-New Delhi (M. K., R.). We thank the CDRI SAIF division for analytical support. CDRI Communication No 10364.",

year = "2022",

month = feb,

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doi = "10.1039/d2cc00257d",

language = "English (US)",

volume = "58",

pages = "3481--3484",

journal = "Chemical Communications",

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T1 - Ru-Catalyzed C–H alkenylation on the arene ring of pirfenidone using pyridone as a directing group

AU - Raziullah, null

AU - Kumar, Mohit

AU - Ahmad, Ashfaq

AU - Dutta, Himangsu Sekhar

AU - Rastogi, Anushka

AU - Gangwar, Manoj Kumar

AU - Koley, Dipankar

N1 - KAUST Repository Item: Exported on 2023-01-12 Acknowledgements: We gratefully acknowledge DST-SERB (EMR/2016/000613) for Financial support, CSIR-New Delhi (H. S. D., A. A., A. R.), and UGC-New Delhi (M. K., R.). We thank the CDRI SAIF division for analytical support. CDRI Communication No 10364.

PY - 2022/2/22

Y1 - 2022/2/22

N2 - A method to functionalize the arene ring of pirfenidone has been demonstrated using pyridone as a directing group.

AB - A method to functionalize the arene ring of pirfenidone has been demonstrated using pyridone as a directing group.

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UR - http://xlink.rsc.org/?DOI=D2CC00257D

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U2 - 10.1039/d2cc00257d

DO - 10.1039/d2cc00257d

M3 - Article

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SN - 1359-7345

VL - 58

SP - 3481

EP - 3484

JO - Chemical Communications

JF - Chemical Communications

IS - 21

ER -

Ru-Catalyzed C–H alkenylation on the arene ring of pirfenidone using pyridone as a directing group

Abstract

Bibliographical note

ASJC Scopus subject areas

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CCDC 2046703: Experimental Crystal Structure Determination :

Cite this

Ru-Catalyzed C–H alkenylation on the arene ring of pirfenidone using pyridone as a directing group

Abstract

Bibliographical note

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Datasets

CCDC 2046703: Experimental Crystal Structure Determination :

Cite this